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Prebiotics in Prevention of Atopy (PIPA)

Primary Purpose

Atopic Dermatitis

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Supplemented Formula
Sponsored by
Federico II University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Atopic Dermatitis

Eligibility Criteria

1 Week - 24 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Gestational age >37 and < 42 weeks.
  2. Birth weight > 2500 gr.
  3. At risk of atopy (see appendix 1).
  4. Informed consent signed by the parents (see appendix 3).

Exclusion Criteria:

  1. Congenital immunodeficiency
  2. Severe congenital disorders or malformations
  3. Born to mother with diabet
  4. Long term intake (> 7 consecutive days) of pro- or prebiotics
  5. Children who have already assumed ≥ 50 mL for feeding bottle of Formulas different from the one object of this study for up to a month.
  6. Parents expected not to be compliant with the study procedures

Sites / Locations

  • University of Padova - Department of Pediatrics

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Placebo Comparator

Active Comparator

Arm Label

Breast Milk

Standard Formula

Supplemented Formula

Arm Description

Breast FED newborns

Standard Formula FED newborns

GOS/PDX Formula FED newborns

Outcomes

Primary Outcome Measures

Cumulative incidence
Cumulative incidence of atopic dermatitis at 36 and 48 weeks

Secondary Outcome Measures

Severity
Severity of atopic dermatitis as judged by the SCORAD score at 36 and 48 weeks and its distribution in three different groups: mild (<15 SCORAD points), moderate (15-40 SCORAD points), and severe (>40 SCORAD points) according to the objective components of the index

Full Information

First Posted
April 15, 2014
Last Updated
April 15, 2014
Sponsor
Federico II University
Collaborators
Mead Johnson Nutrition
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1. Study Identification

Unique Protocol Identification Number
NCT02116452
Brief Title
Prebiotics in Prevention of Atopy
Acronym
PIPA
Official Title
Effects of GOS/PDX Supplemented Formula in Preventing and Modifying the History of Allergy and Acute Infections in a Population of Infants at Risk of Atopy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2011
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federico II University
Collaborators
Mead Johnson Nutrition

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study objective is to evaluate whether a specific prebiotic (GOS/PDX) may have an effect in preventing atopic dermatitis, food allergy, intestinal and/or respiratory infections in infants at risk of atopy. In infants with dermatitis, the hypothesis will be tested that prebiotics reduce the severity of the disease.
Detailed Description
This study is a prospective, double blind, randomised, 24 month study trial comparing formula with 50/50 mixture of GOS/PDX (Enfamil Premium Infant Formula 1 for children <6 months and Formula 2 for children ≥ 6 months) versus standard formula (Enfamil Premium Formula 1 and 2). Study population is composed by newborns at risk for allergy that will be identified at time of delivery. Infants will be eligible if at least one parent or one older sibling have a physician-diagnosed atopic disease (asthma, allergic rhinoconjunctivitis , atopic dermatitis, allergic urticaria, and food allergy as follow described. At time of enrolment (within the first 4 weeks of life) infants will be randomised 1:1 to receive once they will start formula feeding before the day of the 6th month birthday.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
380 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Breast Milk
Arm Type
No Intervention
Arm Description
Breast FED newborns
Arm Title
Standard Formula
Arm Type
Placebo Comparator
Arm Description
Standard Formula FED newborns
Arm Title
Supplemented Formula
Arm Type
Active Comparator
Arm Description
GOS/PDX Formula FED newborns
Intervention Type
Dietary Supplement
Intervention Name(s)
Supplemented Formula
Intervention Description
50:50 mixture of GOS/PDX formula will be administered
Primary Outcome Measure Information:
Title
Cumulative incidence
Description
Cumulative incidence of atopic dermatitis at 36 and 48 weeks
Time Frame
36 - 48 weeks
Secondary Outcome Measure Information:
Title
Severity
Description
Severity of atopic dermatitis as judged by the SCORAD score at 36 and 48 weeks and its distribution in three different groups: mild (<15 SCORAD points), moderate (15-40 SCORAD points), and severe (>40 SCORAD points) according to the objective components of the index
Time Frame
36-48 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Week
Maximum Age & Unit of Time
24 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Gestational age >37 and < 42 weeks. Birth weight > 2500 gr. At risk of atopy (see appendix 1). Informed consent signed by the parents (see appendix 3). Exclusion Criteria: Congenital immunodeficiency Severe congenital disorders or malformations Born to mother with diabet Long term intake (> 7 consecutive days) of pro- or prebiotics Children who have already assumed ≥ 50 mL for feeding bottle of Formulas different from the one object of this study for up to a month. Parents expected not to be compliant with the study procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alfredo Guarino, MD
Organizational Affiliation
University of Naples
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stefania Zanconato, MD
Organizational Affiliation
University of Padova
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Padova - Department of Pediatrics
City
Padova
ZIP/Postal Code
35128
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
29494489
Citation
Ranucci G, Buccigrossi V, Borgia E, Piacentini D, Visentin F, Cantarutti L, Baiardi P, Felisi M, Spagnuolo MI, Zanconato S, Baraldi E, Giaquinto C, Guarino A. Galacto-Oligosaccharide/Polidextrose Enriched Formula Protects against Respiratory Infections in Infants at High Risk of Atopy: A Randomized Clinical Trial. Nutrients. 2018 Mar 1;10(3):286. doi: 10.3390/nu10030286.
Results Reference
derived

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Prebiotics in Prevention of Atopy

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